62 What is Autism?
The intent of the new guidelines is not to reduce qualifying cases but rather
to capture more reliably everyone who merits ASD diagnosis. DSM‐5 is to be
seen as a “living document,” one that can be altered as fresh information comes
to light, for instance regarding two particular groups that require further study
regarding diagnostic norms: infants and adults.
A New ASD Diagnosis Category: Social Communication Disorder
DSM‐5 introduced an additional diagnostic category called SCD. The intent of the
new category is to include individuals who do not exhibit the repetitive behaviors
or severely restricted interests so characteristic of many individuals with classic
autism, and yet have serious deficits in the area of proper use of language in social
settings. Many children can now receive this ASD diagnosis who previously were
diagnosed with PDD‐NOS, a catch‐all category of individuals who were hard to
diagnose under other categories. Those with a previous diagnosis will likely not be
affected by this new category; basically, only newly diagnosed persons will receive
the newly introduced diagnoses from the latest iteration of the DSM.
ASD or a Giant Spectrum of Socioneuropsychological Disorders
Before we get into the fallacy of ASD primarily being a genetic disease and not the
result of environmental exposure to the fetus, it should be noted that until mid‐1970,
the role of genetics and heritability was not mentioned much in the scientific litera-
ture with regards to autism. Let us first look at how we define ASD today.
ASDs affect three different areas of a child’s life:
● Social interaction
● Communication – both verbal and nonverbal
● Behaviors and interests
This so called phenotypic heterogeneity is the hallmark of ASD and why is
that? If ASD was the result of genetic defects, then there would be a common
denominator(s) by which to diagnose the disorders. We will discuss this very
shortly below.
Each child with an ASD diagnosis will have his or her own pattern of autism.
This is a giant loophole in the definition. This will include many children who
have serious chromosomal rearrangements, additions, and deletions as well as
ones with outright well‐defined genetic diseases. This definition is like trying
to put round pegs into square holes!
This definition may include children who are normal but slightly delayed in
their developmental chart. For example, sometimes, a child’s development is